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Cloning and Nucleotide Sequence of a Cyclodextrin Glycosyltransferase Gene from the Alkalophilic Bacillus 1-1

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Proceedings of the Fourth International Symposium on Cyclodextrins

Part of the book series: Advances in Inclusion Science ((AIS,volume 5))

Abstract

A large number of alkalophilic bacteria isolated from soil was screened for cyclodextrin glycosyltransferase activity. The strain 1-1 identified as a member of the Bacillus firmus/lentus group was shown to secrete a cyclodextrin glycosyltransferase which forms mainly β-cyclodextrin, small amounts of γ-cyclodextrin and no α-cyclodextrin. The gene for this enzyme was cloned in E. coli and the nucleotide sequence was determined. The nucleotide sequence reveals an open reading frame of 2109 bp, corresponding to a protein of 703 amino acids (aa). A signal peptide precedes the native polypeptide which differs from all known analogous structures by a negative net charge in its N-terminal part.

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© 1988 Kluwer Academic Publishers

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Schmid, G., Englbrecht, A., Schmid, D. (1988). Cloning and Nucleotide Sequence of a Cyclodextrin Glycosyltransferase Gene from the Alkalophilic Bacillus 1-1. In: Huber, O., Szejtli, J. (eds) Proceedings of the Fourth International Symposium on Cyclodextrins. Advances in Inclusion Science, vol 5. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-2637-0_11

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  • DOI: https://doi.org/10.1007/978-94-009-2637-0_11

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-7690-6

  • Online ISBN: 978-94-009-2637-0

  • eBook Packages: Springer Book Archive

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